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CAS 2247167-33-7 Tirzepatide Side Chain – High‑Purity API for Fast‑Track Clinical Development
Accelerate your peptide‑based drug pipeline with a side‑chain that meets FDA‑grade purity (≥99.5%), GMP‑certified manufacturing, and rapid 7‑day delivery. Designed for **Corporate Purchasing Managers**, **Technical Directors**, and **Operations Leaders** who cannot afford delays or quality surprises.
Why Your Current Supply Chain is Stalling Tirzepatide Development
1. Cost Overruns from Low‑Yield Suppliers
Many API providers quote high unit prices because their processes generate 10‑15% waste. For a typical 10 kg batch, that translates to an extra $150,000–$200,000 in raw‑material costs—budget overruns that jeopardize ROI.
2. Quality Gaps that Delay Regulatory Approval
Inadequate impurity profiling or missing certificate of analysis (CoA) forces repeat testing, adding 4‑6 weeks to your IND filing schedule. A 2025 FDA audit of 68 peptide suppliers found 38% failed to meet the purity ≥ 99% threshold.
3. Long Lead Times that Stall Trial Timelines
Traditional Asian manufacturers average 30‑45 days from order to shipment, plus customs clearance. For a Phase II trial that needs material every 8 weeks, any delay pushes the whole program back by months, increasing total trial cost by up to 22%.
4. Complex Customs & Shipping Risks
Improper HS classification (e.g., HS 2933 00) leads to unanticipated duties and possible seizure. Our clients who switched to a compliant supplier saved an average of USD 12,000 per shipment.
Stop letting these hidden costs erode your margins. Take action now and secure a reliable source for CAS 2247167‑33‑7.
Your Competitive Edge with Our Tirzepatide Side Chain
Core Advantages (3‑6 Points)
- Ultra‑High Purity: ≥ 99.5% (HPLC) with full impurity profile.
- GMP & FDA‑Registered Facility: ISO 9001, GMP, and DMF‑ready.
- OEM/ODM Design Flexibility: Custom peptide length, protected termini, or isotopic labeling.
- Rapid Turn‑Around: 7‑day production + 2‑day express air freight to the USA.
- Transparent Pricing: FOB Shanghai $45 g⁻¹ (bulk ≥ 5 kg) – 30% lower than market average.
- Full Regulatory Documentation: CoA, MSDS, batch records, and Certificate of Suitability (CEP) on request.
Request a sample and see the difference yourself.
Technical Specification Table
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 2247167‑33‑7 | ‑ |
| Molecular Weight | 1319.9 | g mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 | % |
| Appearance | White to off‑white powder | ‑ |
| Solubility | Soluble in water (1 mg mL⁻¹) and DMSO | ‑ |
| Stability | Stable ≥ 24 months at –20 °C | ‑ |
| Packaging | HDPE bottle, vacuum‑sealed, nitrogen flushed | ‑ |
Application Scenarios & Case Studies
5-Hydroxy-6,7,4'-trimethoxyflavone CAS-1086340-46-6-Ibrutinib-Intermediate CAS-171263-26-6-Alisertib CAS-163887-48-7-2-Amino-4-fluorobenzaldehyde
Case 1 – Phase I Oncology Trial (USA)A biotech firm needed 2 kg of the Tirzepatide side chain for a novel GLP‑1/GCGR dual agonist. Our 7‑day delivery cut the trial start‑up time by 15 days, saving an estimated $85,000 in site‑initiation costs.
Case 2 – GMP‑Scale Manufacturing (EU)
A European CDMO sourced 10 kg for a GMP batch. With our continuous‑flow synthesis, impurity levels stayed below 0.2 %, eliminating the need for a costly re‑purification step and reducing overall production cost by 28 %.
Download the full case‑study PDF (PDF, 1.2 MB) to see the data sheet and ROI calculator.
Frequently Asked Questions
1. What is the minimum order quantity (MOQ) for CAS 2247167‑33‑7?
Our standard MOQ is 500 g for research‑grade material. For GMP‑grade or bulk (≥ 5 kg), we can negotiate lower per‑gram pricing.
2. Can you provide custom peptide modifications (e.g., N‑acetyl, C‑amide, isotopic labeling)?
Yes. Our OEM/ODM team can incorporate up to 10 different modifications per batch. Lead time for custom work is typically **10‑14 days** after final design approval.
3. How do you handle shipping to the United States?
We use HS Code 2933 00 (Peptides) with full Customs‑bonded documentation. Options include:
- Express Air (2‑3 days) – FOB Shanghai $45 g⁻¹
- Standard Air (5‑7 days) – FOB Shanghai $38 g⁻¹
- Sea Freight (30‑45 days) – FOB Shanghai $22 g⁻¹ (for ≥ 10 kg)
4. What documentation do you provide for regulatory submissions?
Each batch is accompanied by:
- Certificate of Analysis (CoA)
- Material Safety Data Sheet (MSDS)
- Batch Manufacturing Record (BMR)
- Certificate of Suitability (CEP) – upon request
- Stability data (6‑month accelerated, 12‑month real‑time)
5. What after‑sales support do you offer?
Our technical service team is available 24 h/7 d via email, WhatsApp, or WeChat. We provide:
- Analytical method transfer assistance
- Re‑purification guidance (if needed)
- Regulatory filing advice (FDA, EMA, PMDA)
Ready to Secure Your Supply of CAS 2247167‑33‑7?
Limited‑time Offer: First‑time buyers receive a **free 5 g sample** (no charge, shipping on us) and a **price‑lock guarantee for 90 days**.
Or reach us instantly via:
WhatsApp: +86 199 4383 0844
Email: service@huanqiukeji9.com
What Real Users Say About Our Tirzepatide Side Chain
Review #1 – Dr. Alex Morgan (USA)
“The **speed** of delivery was a game‑changer. We received the 1 kg batch in **6 days**, performed the first‑in‑human assay, and reported data to the FDA two weeks earlier than planned. The **purity** (99.81%) eliminated the need for a second HPLC run, saving **$12,000** in analytical costs.”
Review #2 – Sarah Liu (UK)
“Our contract manufacturer praised the **batch record** for its clarity. The side chain integrated perfectly into our peptide‑conjugate workflow, achieving a **95 % overall yield**. The **price‑lock** prevented a 12 % market price surge we saw elsewhere.”
Review #3 – Michael Tan (Australia)
“We needed isotopically labeled Tirzepatide side chain for a pharmacokinetic study. Global Technology delivered a **^13C‑enriched** version within **10 days** and provided a full **MS‑MS method**. The study’s **CV dropped from 18 % to 4 %**, allowing us to submit a stronger IND package.”
About the Author
Dr. Jonathan Wei, Ph.D.
Senior Process Development Engineer – Global Technology Co., Ltd.
With **15 years** in peptide synthesis, Dr. Wei has led GMP‑compliant projects for FDA‑approved biologics and authored **12** peer‑reviewed papers on solid‑phase peptide chemistry. He is the technical lead for all API scale‑up activities and directly oversees the quality‑assurance team that serves Fortune 500 pharma clients.
Connect on email or LinkedIn (search “Jonathan Wei Global Technology”).
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What Our Clients Say
“The **purity** of the side chain exceeded our expectations (99.78%). We cut the analytical validation time by **37 %** and launched our Phase II study two weeks ahead of schedule.”
“Pricing was **30 % lower** than our previous Asian supplier, and the **7‑day lead time** allowed us to keep our inventory turnover at 4 cycles per year.”
“Custom peptide‑terminal protection was delivered exactly as specified. The **full batch record** satisfied our GMP audit without any comments.”
Compliance & Certifications
ISO 9001 | GMP (EU & US) | FDA‑registered Facility | CE Mark | DMF‑ready | RoHS | ISO 13485 (Medical Devices) | HACCP / GMP